Explain why an amide ion cannot be used to form a carbanion from an alkane in a reaction that favors products. explain why an amide ion cannot be used to form a carbanion from an alkane in a reaction that favors products. the base that would be formed is a weaker base than the alkane (the reactant base). the base that would be formed is a stronger base than the alkane (the reactant base). the acid that would be formed is a stronger acid than the alkane (the reactant acid).
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A5 mole sample of liquid acetone is converted to a gas at 75.0°c. if 628 j are required to raise the temperature of the liquid to the boiling point, 15.600 kj are required to evaporate the liquid, and 712 j are required to raise the final temperature to 75.0°c, what is the total energy required for the conversion?
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What type of reaction is shown below? check all that apply. agno3(aq) + nacl(aq) → nano3(aq) + agcl(s) i synthesis decomposition combustion i single replacement double replacement done
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Explain why an amide ion cannot be used to form a carbanion from an alkane in a reaction that favors...
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